Canonical Allele Identifier: CA1596243778
Gene: GABRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.161882734G= , CM000667.2:g.161882734G= GRCh38
NC_000005.9:g.161309740G= , CM000667.1:g.161309740G= GRCh37
NC_000005.8:g.161242318G= NCBI36
NG_011548.1:g.40544G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393943.10:c.703+33G= MANE Select ENSP00000377517.4:n.703+33G=
ENST00000635880.1:c.703+33G= ENSP00000489738.1:n.703+33G=
ENST00000635916.2:n.2304+33G=
ENST00000636340.1:c.*552+33G= ENSP00000490002.1:n.*552+33G=
ENST00000636408.1:n.507+33G=
ENST00000636573.1:c.703+33G= ENSP00000490320.1:n.703+33G=
ENST00000637044.1:c.*477+33G= ENSP00000490684.1:n.*477+33G=
ENST00000637827.1:c.703+33G= ENSP00000490804.1:n.703+33G=
ENST00000638112.1:c.703+33G= ENSP00000489839.1:n.703+33G=
ENST00000638159.1:c.748+33G= ENSP00000490360.1:n.748+33G=
ENST00000023897.10:c.703+33G= ENSP00000023897.6:n.703+33G=
ENST00000393943.9:c.703+33G= ENSP00000377517.4:n.703+33G=
ENST00000428797.7:c.703+33G= ENSP00000393097.2:n.703+33G=
ENST00000437025.6:c.703+33G= ENSP00000415441.2:n.703+33G=
ENST00000519542.1:n.467+33G=
ENST00000634335.1:c.703+33G= ENSP00000489434.1:n.703+33G=
NM_000806.5:c.703+33G= NP_000797.2:n.703+33G=
NM_001127643.1:c.703+33G= NP_001121115.1:n.703+33G=
NM_001127644.1:c.703+33G= NP_001121116.1:n.703+33G=
NM_001127645.1:c.703+33G= NP_001121117.1:n.703+33G=
NM_001127648.1:c.703+33G= NP_001121120.1:n.703+33G=
NM_001127644.2:c.703+33G= MANE Select NP_001121116.1:n.703+33G=
NM_001127643.2:c.703+33G= NP_001121115.1:n.703+33G=
NM_001127645.2:c.703+33G= NP_001121117.1:n.703+33G=
NM_001127648.2:c.703+33G= NP_001121120.1:n.703+33G=